巨噬细胞
炎症
烧蚀
免疫学
细胞生物学
医学
生物
内科学
生物化学
体外
作者
J.F. Cailhier,Marina Partolina,Srilatha Vuthoori,Shengji Wu,Kyung Ae Ko,Simon J. Watson,John Savill,Jeremy Hughes,Richard A. Lang
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2005-02-15
卷期号:174 (4): 2336-2342
被引量:238
标识
DOI:10.4049/jimmunol.174.4.2336
摘要
Abstract The role played by resident macrophages (Mφ) in the initiation of peritoneal inflammation is currently unclear. We have used a conditional Mφ ablation strategy to determine the role of resident peritoneal Mφ in the regulation of neutrophil (PMN) recruitment in experimental peritonitis. We developed a novel conditional Mφ ablation transgenic mouse (designated CD11bDTR) based upon CD11b promoter-mediated expression of the human diphtheria toxin (DT) receptor. The murine DT receptor binds DT poorly such that expression of the human receptor confers toxin sensitivity. Intraperitoneal injection of minute (nanogram) doses of DT results in rapid and marked ablation of F4/80-positive Mφ populations in the peritoneum as well as the kidney, and ovary. In experimental peritonitis, resident Mφ ablation resulted in a dramatic attenuation of PMN infiltration that was rescued by the adoptive transfer of resident nontransgenic Mφ. Attenuation of PMN infiltration was associated with diminished CXC chemokine production at 1 h. These studies indicate a key role for resident peritoneal Mφ in sensing perturbation to the peritoneal microenvironment and regulating PMN infiltration.
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